Glenoid Resurfacing System and Method

ABSTRACT

A system and method for repairing a defect on an articular surface. An excision guide is positioned on an articular surface, wherein the excision guide includes a guide head and a guide sleeve disposed on the guide head, wherein the guide head includes a contact surface configured to locate the excision guide relative to the articular surface. A guide pin may be advanced through the guide sleeve and secured to the articular surface, wherein the guide sleeve is configured to receive the guide pin therethrough and position the guide pin at an angle β relative to an axis generally normal and central to a defect on the articular surface, wherein angle β is less than 90 degrees.

CROSS-REFERENCE

This application claims the benefit of the filing date of U.S. Provisional No. 61/170,290 filed on Apr. 17, 2009 and U.S. Provisional No. 61/311,605, filed Mar. 8, 2010, the teaching of which are both incorporated by reference herein. This application also relates to Attorney Docket No. ART053, U.S. application Ser. No. ______, filed Apr. 19, 2010, the teachings of which are incorporated herein by reference.

FIELD

This disclosure relates to devices and methods for the repair of defects that occur in articular cartilage on the surface of bones, particularly the shoulder.

BACKGROUND

Articular cartilage, found at the ends of articulating bone in the body, is typically composed of hyaline cartilage, which has many unique properties that allow it to function effectively as a smooth and lubricious load-bearing surface. When injured, however, hyaline cartilage cells are not typically replaced by new hyaline cartilage cells. Healing is dependent upon the occurrence of bleeding from the underlying bone and formation of scar or reparative cartilage called fibrocartilage. While similar, fibrocartilage does not possess the same unique aspects of native hyaline cartilage and tends to be far less durable.

In some cases, it may be necessary or desirable to repair the damaged articular cartilage using an implant. While implants may be successfully used, the implant should have a shape substantially corresponding to the articular cartilage proximate the area where the implant is to be placed in order to maximize the patient's comfort, minimize damage to surrounding areas, and maximize the functional life of the implant.

BRIEF DESCRIPTION OF DRAWINGS

The above-mentioned and other features of this disclosure, and the manner of attaining them, may become more apparent and better understood by reference to the following description of embodiments described herein taken in conjunction with the accompanying drawings, wherein:

FIG. 1 illustrates a side view of an example of an excision device and an implant;

FIG. 2 illustrates a perspective view of an example of an excision device and an implant;

FIG. 3 illustrates an example of an implant;

FIG. 4 illustrates a side view of an example of an implant;

FIG. 5 a illustrates a side view of another example of an implant;

FIG. 5 b illustrates a perspective view of an example of an implant;

FIG. 5 c illustrates a side view of an example of the implant of FIG. 5 b;

FIG. 5 d illustrates another side view of an example of the implant of FIG. 5 b;

FIG. 5 e illustrates a bottom view of an example of the implant FIG. 5 b;

FIG. 5 f illustrates a side perspective view of an example of the implant of FIG. 5 b;

FIG. 5 g illustrates a side perspective view of another example of an implant;

FIG. 6 illustrates an example of a guide pin positioned in the glenoid surface of a scapula;

FIG. 7 illustrates an example of an excision device including a cannulated shaft and a cutter positioned at the distal end of the cannulated shaft passing over the guide pin positioned in the glenoid surface of a scapula;

FIG. 8 illustrates a side view of an example of an excision device including a cannulated shaft and a cutter positioned at the distal end of the cannulated shaft passing over the guide pin positioned in the glenoid surface of a scapula;

FIG. 9 illustrates a side-cross sectional view of an excision device including a cannulated shaft and a cutter positioned at the distal end of the cannulated shaft passing over the guide pin positioned in the glenoid surface of a scapula;

FIG. 10 illustrates a side-cross sectional view of an excision site including an implant;

FIG. 11 illustrates an example wherein a portion of the perimeter of the articular surface is damaged and the guide pin is positioned such that a repair may be made at or near the perimeter of the articular surface;

FIG. 12 illustrates a side-cross sectional view of an excision site including an example of an implant positioned at or near the perimeter of the articular surface; and

FIG. 13 illustrates an example of a side-cross sectional view of an example of an excision site including an example of an implant positioned at or near the perimeter of the articular surface.

FIG. 14 illustrates an example of perspective view of an example of an excision guide and guide pin relative to an articular surface of a glenoid;

FIG. 15 a illustrates an cross-sectional view of the side view of an example of an excision guide having a guide pin positioned therethrough, wherein at least a portion of the guide pin is disposed in an articular surface;

FIG. 15 b illustrates a cross-section view of a side view of an embodiment of an excision guide;

FIG. 15 c illustrates a cross-sectional view of a side view of another embodiment of an excision guide;

FIG. 16 illustrates a cross-sectional side view of an example of a excision device including at least one cutter portioned over a guide pin and relative to the excision guide;

FIG. 17 illustrates a perspective view of an example of an excision guide;

FIG. 18 illustrates a perspective view of an example of an excision device advance over a guide pin;

FIG. 19 illustrates a perspective view of an example of an impact guide received by a guide pin;

FIG. 20 illustrates a perspective view of an example of an impact guide positioned in an excision site and an impact device;

FIG. 21 illustrates a perspective view of another embodiment of an impact guide and an impact device;

FIG. 22 illustrates a perspective view of an example of a secondary excision site provided in the bottom of a first or primary excision site; and

FIG. 23 illustrates an example of a perspective view of an implant positioned in an excision site.

DETAILED DESCRIPTION

According to one embodiment, the present disclosure may feature a system and method for resurfacing at least a portion of an articular surface having a defect by replacing a portion of the articular surface with an implant. The implant may comprise a load bearing surface having a contour and/or shape substantially corresponding to the patient's original articular surface about the defect site which may be configured to engage an adjacent articular surface. The present disclosure will describe a system and method for replacing a portion of the articular surface of the glenoid; however, it should be understood that the system and method according to the present disclosure may also be used to resurface articular surfaces other than the glenoid.

As an initial matter, many of the devices described herein comprise cannulated components configured to be arranged over other components. The degree to which the cannulated passageway (i.e., internal diameter of the passageway/cavity) of a first component corresponds to the external diameter of the component over which it is being placed may be close enough to generally eliminate excessive movement. Excessive movement may be defined as an amount of movement that may result in surgically relevant misalignment of the implant relative to the articular surface.

Referring now to FIG. 1, one embodiment of an excision device 10 and an implant 12 are generally illustrated. As will be explained in greater detail herein, the excision device 10 may be configured to form an implant or excision site within the articular surface (e.g., the glenoid) configured to receive at least a portion of the implant 12. The implant 12 may be configured to replace the articular surface in an area proximate one or more defects. The system and method consistent with the present disclosure may repair a defect on the articular surface of a glenoid without having to replace the entire glenoid.

Accordingly to at least one embodiment, the implant 12 may be configured to replace only a portion of the articular surface proximate the defect site rather than the entire articular surface. As such, the implant 12 may minimize the amount of the articular surface which is operated on thus allowing more of the patient's original articular surface to be unaffected and providing a more physiologically normal joint. The system and method consistent with one embodiment of the present disclosure may allow for “key-hole” surgery in which a minimum number and size of incisions are made. As may be appreciated, “key-hole” surgery may reduce the amount of pain and/or discomfort experienced by the patient and may reduce healing times.

The excision device 10 may include a cannulated shaft 14 defining a passageway 15 configured to be received over at least a portion of a guide pin or the like (not shown). The excision device 10 may also include at least one cutter 16 a, 16 b extending radially outwardly and away from a distal end 18 of the shaft 14. Each cutter 16 a, 16 b may have a cutting surface 20 configured to create a hemispherical implant site, i.e., an excision site to receive the implant. For example, the cutting surface 20 may have a generally arcuate shape which sweeps towards the proximal end of the shaft 14 as the radius R_(e) from the shaft 14 increases on the cutter 16 a, 16 b. It may be appreciated that the hemi-spherical excision site may exhibit some degree of deviation and the hemi-spherical excision site may be, in some examples, teardrop shaped or pyriform.

The contour of the cutting surfaces 20 may define the contours of the excision site as the cutters 16 a, 16 b are rotated about the central axis of the excision site. While the cutting surfaces 20 are illustrated having a generally constant arc or curvature, the cutting surfaces 20 may include one or more protrusions and/or recesses configured to create corresponding radial groove and/or lips/protrusions within the excision site. These radial grooves and/or lips/protrusions on the cutting surfaces 20 may facilitate alignment of the implant 12 and/or may increase the mechanical coupling of the implant 12 within the excision site.

Turning now to FIG. 2, the overall radius R_(e) of the cutters 16 a, 16 b may define the radius of the implant site created by the excision device 10 within the articular surface and may also substantially correspond to the radius R_(i) of the implant 12. In addition, the depth D of the cutters 16 a, 16 b may also define the height of the excision site created by the excision device 10 and may also substantially correspond to the height H of the implant 12. For example, the overall radius R_(e) of the cutters 16 a, 16 b may be between 7.0 mm to 20.0 mm, for example, 7.0 mm to 15.0 mm and/or 10.0 mm to 12.5 mm (including all values and ranges therein) and the depth D may be between 4.0 mm to 10.0 mm, for example, 5 mm (including all values and ranges therein).

According to at least one embodiment, the excision device 10 may include a first and a second cutter 16 a, 16 b which may be disposed approximately 180 degrees relative to each other. For example, the cutters 16 a, 16 b may extend generally radially outwardly from the shaft about a first and a second generally opposite side of the distal end 18 of the shaft 14. The cutters 16 a, 16 b may also have a generally slim profile configured to be disposed between two adjacent articular surfaces as explained further herein. For example, the cutters 16 a, 16 b may have a cross-sectional thickness (t) of 0.5 mm to 3.0 mm, for example, 2.0 mm (including all values and ranges therein). In one embodiment the at least one cutter may provide a generally hemispherical excision site regardless of the angle which the guide pin is disposed relative to the articular surface 54.

The implant 12 may include a load bearing surface 22 and a bone facing surface 24. Turning now to FIG. 3, a top perspective view of an implant 12 consistent with at least one embodiment herein is generally illustrated. The load bearing surface 22 may have a contour substantially corresponding to or based on the contour of the patient's articular surface being replaced (i.e., the articular surface which is removed by the excision device 10). The contour of the load bearing surface 22 may be based on a plurality of measurements taken at the patient's articular surface (for example, using a measuring and/or mapping tool as generally described in U.S. Pat. Nos. 6,520,964, 6,610,067, 6,679,917, 7,029,479 and 7,510,558, which are fully incorporated herein by reference) and/or may be based on one or more templates.

The load bearing surface 22 may be based on two or more curvatures, for example, the anterior-posterior (AP) curvature and the superior-inferior (SI) curvature. One or more of the AP and/or SI curvatures may themselves be based on multiple curves, (for example, as generally described in U.S. patent application Ser. No. 12/027,121, filed Feb. 6, 2008 and entitled SYSTEM AND METHOD FOR JOINT RESURFACE REPAIR, which is fully incorporated herein by reference). The load bearing surface 22 may be generally concaved. For example, the load bearing surface 22 may have a generally hemi-spherical shape.

The load bearing surface 22 may also include a beveled region 26 disposed about the perimeter of the load bearing surface 22. The beveled region 26 may reduce the potential of further damage to the surrounding articular surface by eliminating a hard transition between the load bearing surface 22 and the remaining articular surface. The beveled region 26 may be particularly helpful if a portion of the implant 12 is slightly proud with respect to the remaining articular surface.

The bone facing surface 24 may be configured to be generally received in the excision site created by the excision device 10. For example, the bone facing surface 24 may have a generally hemi-spherical shape substantially corresponding to the contour of the cutting surfaces 20 of the cutters 16 a, 16 b. The bone facing surface 24 may also include one or more lips, protrusions, ribs or the like 28 a-28 n configured to increase the mechanical connection between the implant 12 and the patient's bone within the excision site. Again, these lips or the like 28 a-28 n may generally correspond to the contours of the cutting surfaces 20 of the cutters 16 a, 16 b. The voids or space 30 a-30 n between the lips 28 a-28 n may create pockets for bone in-growth and/or bone cement.

Turning now to FIGS. 4 and 5 a, the implant 12 may optionally include at least one keel or tail 32 extending generally outwardly from the bone facing surface 24. For example, the implant 12 may include at least one keel 32 including a protrusion or button 34 disposed about a distal end of a base region 36 as generally illustrated in FIG. 4. For example, the implant 12 may include a single keel 32 extending generally downwardly and away from the bottom surface 38 of the bone facing surface 24 generally along the central axis C of the implant 12. The base region 36 may be coupled to the bottom surface 38 of the bone facing surface 24 and may have an hour-glass shape which may initially taper radially inwardly and then taper radially outwardly. The bottom surface 33 of the button 34 may have a curvature substantially corresponding to the curvature of the implant site. For example, the bottom surface of the button 34 may have a curvature (generally illustrated by dotted curve D) substantially corresponding to the curvature of the cutting surfaces 20.

The button 34 may extend generally radially outwardly from a distal end of the base region 36. As such, the button 34 may have a diameter D_(b) greater than at least a portion of the base region 36, for example, the portion of the base region adjacent to the button 34. According to one embodiment, the diameter D_(b) of the button 34 may be the same as or slightly larger than the diameter of the cavity in the excision site in which it is configured to be received. As such, the button 34 may form an interference fit with the cavity in the excision site which may secure the implant 12 to the bone and may also facilitate alignment of the implant 12 with respect to the articular surface and the excision site. Alternatively, the diameter D_(b) of the button 34 may be slightly smaller than the diameter of the cavity in which it is configured to be received. As such, the button 34 may also facilitate alignment of the implant 12 with respect to the articular surface and the excision site. In addition, bone cement or the like may be disposed around the keel within the cavity to increase the mechanical connection between the keel 32 and the bone.

FIG. 5 a illustrates another embodiment of a keel 32. The keel 32 may include a base region 36 extending generally outwardly/downwardly and away from the bottom surface 38 of the bone facing surface 24 generally along the central axis C of the implant 12. For example, the keel 32 may extend outwardly/downwardly and away from the bottom surface 38 of the bone facing surface 24 beyond the curvature D substantially corresponding to the curvature of the cutting surfaces 20. The keel 32 may be configured to be received in an additional cavity, pocket or the like formed within the excision site. The additional cavity may be formed subsequent to the formation of the excision site using an additional cutter, chisel, drill or the like (not shown).

The base region 36 may include one or more radial lips, grooves, protrusions or the like 40. The keel 32 may also include a protrusion 42 extending generally downwardly and away from the base portion 36 generally along the central axis C of the implant 12. The protrusion 42 may include one or more radial lips, grooves, protrusions or the like 44 a-44 n. As discussed herein, the keel 32 may be configured to engage a cavity or the like disposed within the excision site and may be configured align the implant 12 with respect to the articular surface and/or the excision site and may also increase the mechanical coupling of the implant 12 to the bone.

While the keels 32 illustrated in FIGS. 4 and 5 a are shown having a generally concentric shape, the keel 32 may have other configurations. For example, in the embodiment illustrated in FIG. 5 b through 5 f the keel 32 and/or the protrusion 42 extending from the keel 32 may have a shape configured to prevent rotations of the implant 12 with respect to the articular surface. The keel 32 may have a non-circular shape configured to be received in the excision site in a lock-and-key configuration. By way of example, the keel 32 may have a generally multifaceted geometry (such as, but not limited to, rectangular, pentagonal, hexagonal or the like) configured to received in the excision site. Similarly, the protrusion 42 may exhibit a multifaceted geometry such as generally oblong or rectangular, pentagonal, hexagonal, or the like. The protrusion 42 may also exhibit an additional (or second) protrusion 44 a extending outwardly in a radial direction from the central axis of the implant 12, which may form a raised edge or surface around the perimeter of the protrusion 42. As illustrated, protrusion 42 may end in a relatively pointed tip, or may exhibit a curvature as illustrated in FIG. 5 a. FIG. 5 g illustrates a further embodiment of protrusion 42, wherein the protrusion 42 may be formed from a variety of features, such as circular, rectangular, etc. It may be appreciated that, the implant 12 and the keel 32 may be a single, integral or unitary component or may be formed from two or more pieces which may be secured to each other (either permanently or removably secured).

Turning now to FIGS. 6-10, one method of installing an implant 12 consistent with the present disclosure is generally illustrated. One or more incisions 49 may be created proximate the patient's shoulder 50 to provide access to the defect 52 on the patient's articular surface 54, for example, using a scalpel or the like. The incision 49 may be made through the anterior portion of the patient. Again, the present disclosure will describe a system and method for replacing a portion of the articular surface of the glenoid; however, it should be understood that the system and method according to the present disclosure may also be used to resurface articular surfaces other than the glenoid. The system and method consistent with one embodiment of the present disclosure may allow for “key-hole” surgery in which a minimum number and size of incisions are made. As may be appreciated, “key-hole” surgery may reduce the amount of pain and/or discomfort experienced by the patient and may reduce healing times.

Once the incision is created, a guide pin 56, FIG. 6, may be positioned about the glenoid 58 on the scapula 60 to provide an access passageway to the glenoidal articular surface 54 as will be described herein. Consistent with one embodiment, the guide pin 56 may comprise threaded and/or self-tapping tip (not shown) configured to be secured to the patient's bone. The guide pin 56 may be secured to the bone using a drill or the like (not shown) and at least a portion of which may be disposed proximate to and/or within the defect site 52 on the articular surface 54. Optionally, a drill guide (not shown) may be used to facilitate alignment of the guide pin 56 with respect to the articular surface 54.

The guide pin 56 may be disposed at an angle α relative to the articular surface 54. Angle α may be less than or equal to 90 degrees, wherein α≦90 degrees with respect to the articular surface 54. In some examples, angle α may be less or equal to 90 degrees and greater than or equal to 45 degrees with respect to the articular surface 54, wherein 45 degrees ≦α≦90 degrees with respect to the articular surface 54. In further examples, 90 degrees >α>45 degrees and/or 90 degrees >α≧45 degrees, with respect to the articular surface 54. The degree of the angle α may depend on the location and/or size of the defect 52 and may be selected to avoid contact with the humerus 62. In some circumstances, the degree of the angle α may also be selected to avoid contact with the perimeter of the articular surface 54.

Once the guide pin 56 is secured to the articular surface 54, the excision device 10 may be advanced over the guide pin 56 as generally illustrated in FIG. 7. For example, the guide pin 56 may be received within the passageway 15 defined by the cannulated shaft 14. According to at least one embodiment, the cutters 16 a, 16 b may be generally aligned in a single plane extending along the longitudinal axis of the excision device 10. The plane of the cutters 16 a, 16 b may be orientated generally tangential to the articular surface 64 of the humerus 62 such that the cutters 16 a, 16 b may slide by the articular surface 64 of the humerus 62 and between the humerus 62 and the scapula 60 as generally illustrated in FIGS. 7 and 8.

Once the cutters 16 a, 16 b are advanced over the guide pin 56 to the articular surface 54, the excision device 10 may be rotated about the guide pin 56. As may be best seen in FIG. 8, a pocket of cavity 66 may be present between the articular surface 54 of the glenoid 58 and the articular surface 64 of the humerus 62. The cutters 16 a, 16 b of the excision device 10 may therefore rotate about the guide pin 56 without contacting the articular surface 64 of the humerus 62. The cutters 16 a, 16 b may have generally flat cutting surfaces 20, forming a point along the length thereof, or may have serrated cutting surfaces.

The excision device 10 may thus be rotated about the guide pin 56 to form an excision site 70 within the articular surface 54 of the glenoid 60 as generally illustrated in FIG. 9. Due to the contour of the cutting surfaces 20 of the cutters 16 a, 16 b, the excision site 70 created by the excision device 10 may have a generally hemi-spherical configuration regardless of the angle α of the guide pin 56.

Once the excision site 70 is formed within the articular surface 54, the excision device 10 and the guide pin 56 may be removed as generally illustrated in FIG. 10. The removal of the guide pin 56 may leave a cavity 72 formed by the distal tip of the guide pin 56. The implant 12 may then be received in the excision site 70. The spherical configuration of the excision site 70 may normalize the implant 12 with respect to the remaining articular surface 54. The load bearing surface 22 of the implant 12 may substantially match the original contour of the patient's articular surface 54 which was removed.

As illustrated in FIG. 11, the system and method according to the present disclosure may also repair a defect 80 on the articular surface 54 in which a portion of the perimeter of the articular surface 54 is damaged or missing. For example, the posterior portion P of the articular surface 54 may have a defect 80 wherein a portion of the perimeter of the articular surface 54 is missing which may be caused by advanced chronic shoulder dislocation and/or early onset arthritis. To repair a defect 80 proximate the perimeter of the articular surface 54, the guide pin 56 may be moved further towards the posterior end P of the articular surface 54. The exact location of the guide pin 56 with respect to the articular surface 54 may depend on the location and size of the defect 80 as well as the size of the cutters 16 a, 16 b of the excision device 10.

According to one embodiment, the guide pin 56 may be located a distance away from the perimeter of the articular surface 54 which generally corresponds to the radius R_(e) of the cutters 16 a, 16 b. The excision device 10 may be advanced over the guide pin 56 and rotated as described herein. Accordingly, the cutters 16 a, 16 b may remove a portion of the articular surface 54 to form an excision site 81 disposed about the perimeter of the articular surface 54 as generally illustrated in FIG. 12. The excision device 10 and the guide pin 56 may then be removed and the implant 12 may be received within the excision site 81. As may be seen in FIG. 12, a portion of the implant 12 may replace the perimeter of the articular surface 54 which was damaged and/or missing.

The implant 12 may also include a keel 32 as generally illustrated in FIGS. 12 and 13. The keel 32 may facilitate alignment of the implant 12 with respect to the articular surface 54 and/or may provide an increased mechanical connection between the implant 12 and the bone. As discussed herein, the excision site 81 may also include one or more cavities 83, FIG. 13, configured to received at least a portion of the keel 32 (for example, but not limited to, one or more radial lips 44 a-44 n of the protrusion 42.

Once the position/orientation of the implant 12 has been confirmed (i.e., the contour of the load bearing surface 22 has been confirmed along the AP and/or SI planes to generally correspond to the original contour of the articular surface), the implant 12 may be secured to the bone. The implant 12 may be held in place by the lips, protrusions, ribs or the like 28 a-28 n of the bone facing surface 24, the keel 32, and/or bone cement or the like.

Turning to FIGS. 14-21, one system and/or method for locating an implant 12 consistent with the present disclosure is generally illustrated. The description of the system and methods herein are not limited to the treatment of any single articular surface of the glenoid and may apply not only to the one or more articular surfaces that may be present in the glenoid but to other articular surfaces through out the body as well.

One or more incisions 49 may be created proximate to the patient's shoulder 50 to provide access to the defect on the patient's articular surface 54, using, for example, a scalpel or the like. As may be appreciated, the glenoid may include one or more articular surfaces 54. Each of the articular surfaces may define a concavity as illustrated in FIG. 14 a.

A portion of an excision guide 102 may be positioned within the incision and located between the humerus 62 and the articular surface 54 of the glenoid 58. The excision guide may include an arm 104 and a head 106, which may, in some embodiments, be inserted through the incision in such a manner to avoid contact with the humerus 62. FIGS. 14 b and c illustrate embodiments of the excision guide head 106 and, in particular, variations in the contact surfaces 116 of the excision guide head 106 located on the lower portion 117 of the excision guide head 106. For example, in one embodiment, illustrated in FIG. 14 b, the contact surface 116 may generally conform to the articular surface 54. In another embodiment, illustrated in FIG. 14 c, the contact surface 116 may be a ring near the periphery of the lower portion 117 of the excision guide head 106. As may be appreciated in some embodiments, when in the shape of a ring, the contact surface may be continuous or may, in other embodiments, be discontinuous forming ridges around the contact surface 116. The excision guide 102 may also include a handle 108, which may or may not include one or more indentations 110 to assist in manipulation and/or stabilization of the excision guide 102. The handle may be affixed to the upper portion of the excision guide head 119.

The head 106 of the excision guide 102 may be located over a defect 52 of an articular surface 54. The head 106 may locate the excision guide 102 relative to the articular surface 54. In some embodiments, the head 106 may be generally centered on the articular surface 54 including the defect 52. For example, in one embodiment, the head 106 may be located generally centered in the concavity 55 of the articular surface 54. Once the head 106 is positioned over the defect 52, the guide pin 56 may be received into and pass through a guide sleeve 112 disposed on the head 106. As illustrated in FIGS. 14 b and c, the guide sleeve 112 may define an opening from the upper surface 119 of the excision guide head 106 through the lower surface 117 of the excision guide head 106. The guide sleeve 112 may position the guide pin 56 relative to the defect 52 on the articular surface. In addition, the guide sleeve 112 may be formed in and/or integral to the head 106 or may be formed in an insert connected to the head 106.

As illustrated in FIG. 15, the excision guide 102 may orient the working axis (W) of the guide pin 56 in one or more planes. For example, in one aspect, the guide sleeve 112 may angle the guide pin 56, such that the guide pin may be positioned at an angle α that may be 90 degrees or less from the articular surface, including all values and increments in the range of 10 degrees to 90 degrees, such as in one embodiment 45 degrees to 75 degrees or in a further embodiment 60 degrees from the articular surface 54.

In another aspect, the guide sleeve 112 of the excision guide 102 may orient the working axis (W) of the guide pin 56 at an angle β relative to a normal axis (N). The normal axis (N) may, in some embodiments, be generally normal and central to a defect 80 in the articular surface 54. Angle β may be 90 degrees or less and in some examples, including all values and increments in the range of 5 degrees and 80 degrees, such as in the range of 10 degrees to 30 degrees. FIG. 16 illustrates another example of the working axis (W) defined by the guide sleeve 112 to an axis (N) generally central and normal to the lowest point of the contact surface 116 of the excision guide head 106, which may correspond to the axis generally normal and centrally located to defect 80 or to the deepest point of the excision site 70.

The guide sleeve 112 may also offset the intended entry point 114 of the guide pin 56 in the articular surface 54 radially outward from the axis (N) normal and generally central to the excision site and/or the articular surface 54. FIG. 17 illustrates an embodiment of the positioning of the at least one cutter 16 a, 16 b relative to the positioning of the excision guide 102. In one embodiment, the offset (O) may be determined based on the angle of entry of the guide pin 56 (α or β) into the articular surface 54 and/or the depth of the desired excision site, or the height of the desired implant. For example, the offset (O) may be proportional to the angle α of the guide pin 56 to the articular surface 54 or angle β of the guide pin 56 to the normal axis (N).

The working axis (W) may be positioned at an angle β in the range of 10 degrees to 90 degrees, such as in one embodiment, 15 degrees to 45 degrees, or in a further embodiment 60 degrees from the normal axis (N). As may be appreciated, in some embodiments, the surface of the excision guide head 116 may exhibit some degree of curvature and may be convex. The curvature of the surface of the excision guide head 116 may be configured to generally match the curvature of at least a portion of the articular surface 54. In some embodiments, it may be appreciated, that the curvature of the articular surface 54 and the surface of the excision guide head may not match exactly but may provide a “close fit” sufficient to locate the excision guide head 106 within the glenoid 58. In some non-limiting embodiments, the curvature of the excision guide head surface 116 may be generally hemispherical, including pyriform or teardrop in shape.

Once the guide pin 56 is positioned in the articular surface 54 of the glenoid 58, as illustrated in FIG. 15, the excision guide 102 may be removed from the glenoid 58 by sliding the excision guide 102 up the guide pin 56 away from the glenoid 58. As illustrated in FIG. 18, the excision device 10, including one or more cutters 16 a and 16 b, may be slid (in direction of arrow) over the guide pin 56 and, as described above, the excision device 10 may be rotated forming an excision site 70 in the articular surface 54.

The excision device 10 may then be removed from the guide pin 56 and an impact guide 120 may be inserted through the incision 49 and over the guide pin 56, an embodiment of which is illustrated in FIGS. 19 a through 19 c. The impact guide 120 may include an impact guide arm 122, an impact guide head 124 and an impact guide handle 126. In one embodiment, the impact guide 120 may be the same as the excision guide 102, wherein the head 106 of the excision guide 102 may be interchangeable with the one or more impact guide heads 124. In another embodiment, the impact guide 120 may be separately provided from the excision guide 102.

As may be appreciated, the impact guide heads 124 may generally correspond to or mimic the size and shape of an implant, described above. An embodiment of an impact guide head is illustrated in FIG. 19 b, wherein the impact guide head 124 may include a lower portion 125 that substantially conforms to the generally hemispherical excision site. The impact guide head may exhibit a given height H_(t) and radius R_(t) matching that of an implant to be provided in the excision site 70 (see FIG. 19 a). In another embodiment, illustrated in FIG. 19 c, the impact guide may include a lower portion 127 that includes a ring or bevel around the periphery that may conform to the excision site. The remainder of the lower portion 125 may be recessed.

The impact guide head 124 may include a guide notch 128, which may be inserted over the guide pin 56 or around the guide pin 56 (as illustrated in FIG. 19 a). It may be appreciated that while a notch is illustrated defining an opening in the periphery of the impact guide head 124, i.e., extending to the periphery of the impact guide head 124, the guide notch 128 may also include a sleeve defined in the impact guide head 124. As illustrated in FIGS. 19 b and 19 c, the guide notch 128 may generally define an opening from the upper portion 127 through the lower portion 125 of the impact guide head 124. In addition, the guide notch 128 may include at least one surface 129 that may accommodate the angle and offset of the guide pin 56 relative to the articular surface 54, such that the impact guide head 124 may be positioned generally central within the excision site 70 and the guide pin 56 may rest on the surface 129.

Upon placement of the impact guide head 124 by the impact guide 120 into the excision site 70, a determination may be made as to whether the excision site 70 is sufficiently deep enough to accommodate the implant that may eventually be placed within the excision 70. As may be appreciated, if the excision site 70 is not sufficient deep, or properly formed, the impact guide 120 may be removed from the excision site 70 and the guide pin 56. The excision device 10 may again be placed over the guide pin 56 and further excision may be provided to deepen or further form the excision site 70. This procedure of checking the excision site 70 using the impact guide head 124 may be repeated until it is determined that an implant will fit within the excision site 70. In some embodiments, the use of the impact guide 120 may be to prevent the implant from being too proud in the excision site and from rising above the articular surface 54. In other embodiments, the impact guide head 124 and/or the impact guide 120, may be interchanged with one or more impact guide heads and/or impact guides to determine which implant may better fit or accommodate the excision site in terms of the implant radius or height. Accordingly, one or more impact guide heads 124 may be provided. In some embodiments, the impact guide heads 124 may be interchangeable and removable from the impact guide 120. In other embodiments, a number of impact guides 120 may be provided including different sized impact guide heads 124 fixed to the impact guide 120.

Once an impact guide has been selected based on, for example, the size of the excision site, the impact guide head 124 may be seated in the excision site 70 as illustrated in the embodiment of FIG. 20. In one embodiment, the guide pin 56 may optionally be removed before or after seating the selected impact guide head 124. The impact guide head 124 may include an impact slot 130 defined therein. As illustrated in FIG. 20, the impact slot 130 is generally rectangular in cross-section; however, as may be appreciated, other cross-sectional geometries may be provided, such as circular, as illustrated in FIG. 21, as well as elliptical shaped, square shaped, etc. An impact device 132, such as a chisel, punch or awl may be provided, the distal end 134 of which may fit in and extend through the impact slot 130. Therefore, in some embodiments, the distal end may be longer than the length of the impact slot. In addition, the distal end of the impact device 132 may exhibit a cross-sectional area that may be slightly smaller than that of the impact slot 130. The proximal end 136 of the impact device 132 may provide a striking surface 138, which may be hit by hand, or with a hammer or other device, causing the impact device 132 to extend through the impact slot 130 creating a secondary excision site 140 in the primary or first excision site 70. In some embodiments, the impact device may include a sagittal saw or other cutting device, which may be inserted through the impact slot 130. If the guide pin 56 has not yet been removed, it may be removed at this time.

While the proximal end 136 of the impact device 132 is illustrated in FIG. 20 as being provided at an angle γ to the arm 122 of the impact guide 120, wherein angle γ may be in the range of 15 degrees to 120 degrees, including all values and increments therein, in some embodiments, the impact device 132 may be inserted closer to the impact guide 120, wherein angle γ may be in the range of 0 degrees to 45 degrees, including all values and increments therein. In other embodiments, the proximal portion 136 of the impact device may be generally parallel to the arm 122 of the impact guide 120. In such a manner, the impact device 132 may be inserted into incision 49 in the patient (FIG. 6) without the need for expanding the size of the incision 49 greater than necessary to accommodate the head of the excision guide or the head of the impact guide. Further, the impact device 132 may include a curvature 137, which may generally fit over the curvature 123 of the arm 122 of the impact guide 120.

FIG. 22 illustrates an embodiment of a secondary excision site 140 provided in an excision site 70. The secondary excision site 140 is illustrated as being generally rectangular; other cross-sectional geometries may be provided as well. In addition, the depth D_(s) of the secondary excision site (illustrated in broken lines) may be formed to generally correspond with protrusions 34, 42, 44 a-d that may extend from the keel 32 of the bone facing surface of the implant 12, illustrated in the embodiments of FIGS. 4 and 5 a-f.

While the implant 12 may be held in place in some examples through a mechanical fit, such as through an interference fitbone adhesive may be used to secure the implant 12 in place in other embodiments. In such a manner a layer of bone adhesive may be delivered to the excision site 70, and optionally to the secondary excision site 140 and the implant 12 may be situated over the adhesive and positioned within the excision site.

Accordingly, an aspect of the present disclosure relates to a system for repairing a defect on a patient's articular surface. The system may include a guide pin configured to be secured into an articular surface of a glenoid, an excision guide and an excision device.

The excision guide may include a guide head wherein the guide head includes a contact surface configured to locate the excision guide relative to the articular surface. In some embodiments, the guide head may be configured to be positioned generally central on the articular surface. The excision guide may also include a guide sleeve disposed on the guide head. The guide sleeve may be configured to receive the guide pin therethrough and position the guide pin at an angle β relative to an axis generally normal and central to a defect on the articular surface, wherein angle β is less than 90 degrees. In some embodiments, angle β may be in the range of 10 degrees to 90 degrees. In further embodiments, angle β may be in the range of 10 degrees to 30 degrees. The guide sleeve may also be configured to radially offset a point of entry the guide pin into the articular surface from the axis. The excision guide may further include an excision guide arm affixed to the guide head and a handle affixed to the guide arm.

The excision device may include a cannulated shaft and at least one cutter. The cannulated shaft may be configured to be advanced over the guide pin. The at least one cutter may be configured to form a generally hemi-spherical excision site in the articular surface.

A further aspect of the present disclosure relates to a system for repairing a defect on a patient's articular surface. The system may include a guide pin configured to be secured into an articular surface of a glenoid, an impact guide and an impact device.

The impact guide may include an impact guide head having an upper portion and a lower portion. In some embodiments, the impact guide head may have a height Ht that corresponds to a height H of an implant configured to be received in the excision site. In some embodiments, the impact guide head may have a radius Rt that corresponds to a radius Ri of an implant configured to be received in the excision site. In further embodiments, the impact guide head may be releasably coupled to an impact guide arm.

The impact guide head may also have a guide notch defining a first opening through the impact guide head from the upper portion to the lower portion of the impact guide head. The impact guide head may also include a periphery and the first opening may extend to the periphery. The guide notch may be configured to receive the guide pin.

The impact guide may also include an impact slot defining a second opening through the impact guide head from the upper portion of the impact guide head to the lower portion of the impact guide head. The lower portion of the guide head may be configured to be received in an excision site of the articular surface.

The impact device may be configured to be received in and extend through the impact slot. The impact device may include a proximal end and a distal end, wherein the proximal end includes a striking surface and the distal end is configured to be received in and extend through the impact slot. In some embodiments, the impact device may include a chisel. The impact device may be positioned at an angle γ relative to the impact guide arm, wherein angle γ is in the range 0 degrees to 45 degrees. The impact guide may also includes an impact guide arm and the impact device may include a proximal end and a distal end, and the proximal end of the impact device may be configured to be disposed generally parallel to the impact guide arm when the distal end is received in the impact slot.

Another aspect of the present disclosure relates to a method for repairing a defect on a patient's articular surface. The method may include positioning on an articular surface an excision guide, wherein the excision guide includes a guide head and a guide sleeve disposed on the guide head, wherein the guide head may includes a contact surface configured to locate the excision guide relative to the articular surface. The method may also include advancing a guide pin through the guide sleeve, wherein the guide sleeve is configured to receive the guide pin therethrough and position the guide pin at an angle β relative to an axis generally normal and central to a defect on the articular surface, wherein angle β is less than 90 degrees. The guide pin may then be secured to the articular surface.

The method may also include advancing an excision device over the guide pin, wherein the excision device includes a cannulated shaft and at least one cutter. A generally hemi-spherical excision site may be formed in the articular surface with the cutter. A secondary excision site may also be formed within the generally hemi-spherical excision site in which a portion of the implant may be positioned.

In some embodiments, the method may include advancing an impact guide over the guide pin, wherein the impact guide includes an impact guide head, a guide notch defined in the impact guide head and an impact slot defined in the impact guide head, wherein the guide notch may be configured to receive the guide pin. The impact guide head may then be located in the excision site.

As mentioned above, the present disclosure is not intended to be limited to a system or method which must satisfy one or more of any stated or implied object or feature of the present disclosure and should not be limited to the preferred, exemplary, or primary embodiment(s) described herein. The foregoing description of a preferred embodiment of the present disclosure has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the present disclosure to the precise form disclosed. Obvious modifications or variations are possible in light of the above teachings. The embodiment was chosen and described to provide the best illustration of the principles of the present disclosure and its practical application to thereby enable one of ordinary skill in the art to utilize the present disclosure in various embodiments and with various modifications as is suited to the particular use contemplated. All such modifications and variations are within the scope of the present disclosure. 

1. A system for repairing a defect on a portion of an articular surface of a patient's glenoid, said system comprising: a guide pin configured to be secured into said articular surface of said glenoid proximate to said defect; an excision guide including a guide head and a guide sleeve disposed through said guide head, wherein said guide head includes a contact surface configured to locate said excision guide relative to said articular surface and said guide sleeve is configured to receive said guide pin therethrough and position said guide pin at an angle β relative to an axis generally normal and central to said defect on said articular surface, wherein angle β is less than 90 degrees; and an excision device, wherein said excision device includes a cannulated shaft and at least one cutter generally aligned in a single plane extending along a longitudinal axis of said cannulated shaft, wherein said cannulated shaft is configured to be advanced over said guide pin and said at least one cutter is configured to form a generally hemi-spherical excision site in said articular surface.
 2. The system of claim 1, wherein angle β is selected to avoid contact with a corresponding humerous.
 3. The system of claim 1, wherein angle β is in the range of 10 degrees to 90 degrees.
 4. The system of claim 1, wherein angle β is in the range of 10 degrees to 30 degrees.
 5. The system of claim 1, wherein said guide sleeve is configured to radially offset a point of entry of said guide pin into said articular surface from said axis.
 6. The system of claim 1, wherein said excision guide further includes an excision guide arm affixed to said guide head and a handle affixed to said guide arm.
 7. A system for repairing a defect on a portion of an articular surface of a patient's glenoid, said system comprising: a guide pin configured to be secured into said articular surface of said glenoid proximate to said defect; an impact guide including: an impact guide head having an upper portion and a lower portion, said lower portion configured to be received in a primary excision site of said articular surface, a guide notch defining a first opening through said impact guide head from said upper portion to said lower portion, wherein said guide notch is configured to receive said guide pin, and an impact slot defining a second opening through said impact guide head from said upper portion to said lower portion, an impact device configured to be received in and extend through said impact slot to form a secondary excision site in said primary excision site.
 8. The system of claim 7, wherein said impact guide head includes a periphery and said first opening extends to said periphery.
 9. The system of claim 7, wherein said impact guide head is releasably coupled to an impact guide arm.
 10. The system of claim 7, wherein said impact guide head has a height Ht that corresponds to a height H of an implant configured to be received in said primary excision site.
 11. The system of claim 7, wherein said impact guide head has a radius Rt that corresponds to a radius Ri of an implant configured to be received in said excision site.
 12. The system of claim 7, wherein said impact device includes a proximal end and a distal end, wherein the proximal end includes a striking surface and said distal end is configured to be received in and extend through said impact slot.
 13. The system of claim 7, wherein said impact device includes a chisel.
 14. The system of claim 7, wherein said impact device is positioned at an angle γ relative to the impact guide arm, wherein angle γ is in the range 0 degrees to 45 degrees.
 15. The system of claim 7, wherein said impact guide includes an impact guide arm and said impact device includes a proximal end and a distal end, and said proximal end of said impact device is configured to be disposed generally parallel to said impact guide arm when said distal end is received in said impact slot.
 16. A method for repairing a defect on a portion of an articular surface of a patient's glenoid, said system comprising: positioning an excision guide on said articular surface proximate to said defect, wherein said excision guide includes a guide head and a guide sleeve disposed through said guide head, wherein said guide head includes a contact surface configured to locate said excision guide relative to said articular surface; advancing a guide pin through said guide sleeve, wherein said guide sleeve is configured to receive said guide pin therethrough and position said guide pin at an angle β relative to an axis generally normal and central to said defect on said articular surface, wherein angle β is less than 90 degrees; securing said guide pin to said articular surface; and advancing an excision device over said guide pin to form a generally hemi-spherical primary excision site in said articular surface, wherein said excision device includes a cannulated shaft and at least one cutter generally aligned in a single plane extending along a longitudinal axis of said cannulated shaft; and
 17. The method of claim 16, further comprising forming a secondary excision site within said generally hemi-spherical primary excision site.
 18. The method of claim 17, further comprising positioning a portion of said implant into said secondary excision site.
 19. The method of claim 16, further comprising: advancing an impact guide over said guide pin into said generally hemi-spherical primary excision site, wherein said impact guide includes an impact guide head, a guide notch defined in said impact guide head and an impact slot defined in said impact guide head, wherein said guide notch is configured to receive said guide pin; and advancing an impact device through said impact slot to form a secondary excision site in said primary excision site.
 20. The method of claim 16, wherein angle β is selected to avoid contact with a corresponding humerous. 